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首页> 外文期刊>Genes and genomics >Whole-genome association study for the roan coat color in an intercrossed pig population between Landrace and Korean native pig
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Whole-genome association study for the roan coat color in an intercrossed pig population between Landrace and Korean native pig

机译:全基因组关联研究在长白猪和韩国本地猪之间的杂交猪种群中的软皮毛颜色

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The roan coat color is characterized by white hairs intermingled with colored hairs. Candidate genes based on comparative phenotypes in horses and cattle involve the KIT and KIT ligand (MGF) genes. Here, we report the result of the whole genome scanning to detect genomic regions responsible for the roan coat color, using a three-generation pedigree of 62 pigs in an intercross between Landrace and Korean native pig. These pigs were genotyped using the PorcineSNP 60 BeadChip (Illumina, USA). The wholegenome scan indicated that three genomic regions, 35-36 Mb, 38-39 Mb, and 58-59 Mb on SSC8, were commonly and highly associated/linked with the roan phenotype in the case/control, sib-pair, and linkage test, respectively. The porcine KIT was selected asa candidate gene, because it is located in one of the three significant regions and its function is related to coat color formation. SNPs and hidels within coding sequence (CDS), promoter, and 3'-UTR of KIT were surveyed. Twenty-two SNPs in the CDS reported previously, as well as nine variations in promoter (2 SNPs) and 3'-UTR (5 SNPs and 2 Indels) were detected. Although no causative mutations were identified, these results will help to elucidate the genetic mechanisms involved in the expression of theroan phenotype and will aid in identifying key mutations responsible for the roan phenotype in further studies.
机译:an色的特征是白发与有色的头发混在一起。在马和牛中基于比较表型的候选基因涉及KIT和KIT配体(MGF)基因。在这里,我们报告了全基因组扫描的结果,以使用长白猪和韩国本地猪之间的杂交的62头猪的三代谱系,检测了造成软皮毛颜色的基因组区域。使用PorcineSNP 60 BeadChip(Illumina,美国)对这些猪进行基因分型。全基因组扫描表明,在病例/对照,同胞对和连锁中,SSC8上的三个基因组区域(35-36 Mb,38-39 Mb和58-59 Mb)与roan表型通常且高度相关/关联。测试。猪KIT被选为候选基因,因为它位于三个重要区域之一中,并且其功能与毛色形成有关。调查了KIT的编码序列(CDS),启动子和3'-UTR内的SNP和细胞。先前报道的CDS中有22个SNP,以及启动子(2个SNP)和3'-UTR(5个SNP和2个Indel)的9个变异。尽管未鉴定出致病突变,但这些结果将有助于阐明涉及theroan表型表达的遗传机制,并将有助于在进一步的研究中鉴定负责roan表型的关键突变。

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